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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216879Generated: October 29, 2026

Carbon Tetrachloride → HCID 57708010, compound

https://huagongshe.com/reaction/216879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantBenzoyl PeroxideHCID 7187—
ReactantHCID 57707832HCID 57707832—
ReactantHCID 57707833HCID 57707833—
ProductHCID 57708010HCID 57708010—
ProductHCID 57708058HCID 57708058—

Reaction Steps

A mixture of 5-chloro-2-(3-fluorophenyl)-3-isopropylquinoxaline and 5-chloro-3-(3-fluorophenyl)-2-isopropylquinoxaline (3.3042 g, 10.99 mmol) and 1,3-dibromo-5,5-dimethylhydantoin (4.712 g, 16.48 mmol) were suspended in carbon tetrachloride (109.9 mL, 10.99 mmol). To the mixture was added benzoyl peroxide (0.3548 g, 1.099 mmol) and the mixture was heated at reflux. After 20 h, the mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel column chromatography on a 120 g of Redi-Sep™ column using 0 to 10% gradient of EtOAc in hexane over 15 min and then 10% isocratic of EtOAc for 30 min as eluent to give 3-(2-bromopropan-2-yl)-5-chloro-2-(3-fluorophenyl)quinoxaline and 2-(2-bromopropan-2-yl)-5-chloro-3-(3-fluorophenyl)quinoxaline as a yellow solid: LC-MS (ESI) m/z 379.0 and 381.0 [M+H]+. The mixture of two regioisomers was carried as a mixture without further purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193199B2
Source datasetuspto-grants-2012_06
ORD IDord-28566c94aa054a27bb05c56f56bbb7f6
Source noteuspto-grants-2012_06